| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000344327 |
| Start |
101583431:101583431(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.73C>T |
| AA Mutation |
p.Arg25Cys(p.R25C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000344327 |
| Start |
101471258:101471258(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2334G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000344327 |
| Start |
101504117:101504117(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs778214024
|
| CDS Mutation |
c.852T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |